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1. (Article ID: 5307)
Liu J, Wang X, Pu H, Liu S, Kan J, Jin C
Recent advances in endophytic exopolysaccharides: Production, structural characterization, physiological role and biological activity
Carbohydrate Polymers 157 (2017)
1113-1124
Endophytes are microorganisms that colonize living, internal tissues of plants without causing any immediate, overt negative effects. In recent years, both endophytic bacteria and fungi have been demonstrated to be excellent exopolysaccharides (EPS) producers. This review focuses on the recent advances in EPS produced by endophytes, including its production, isolation and purification, structural characterization, physiological role and biological activity. In general, EPS production is influenced by media components and cultivation conditions. The structures of purified EPS range from linear homopolysaccharides to highly branched heteropolysaccharides. These structurally novel EPS not only play important roles in plant-endophyte interactions; but also exhibit several biological functions, such as antioxidant, antitumor, anti-inflammatory, anti-allergic and prebiotic activities. In order to utilize endophytic EPS on an industrial scale, both yield and productivity enhancement strategies are required at several levels. Besides, the exact mechanisms on the physiological roles and biological functions of EPS should be elucidated in future.
exopolysaccharides, biological activity, Structural characterization, endophytes, physiological role
NCBI PubMed ID: 27987813Publication DOI: 10.1016/j.carbpol.2016.10.084Journal NLM ID: 8307156Publisher: Elsevier
Correspondence: junliu

yzu.edu.cn
Institutions: College of Food Science and Engineering, Yangzhou University, Yangzhou, China
The publication contains the following compound(s):
- Compound ID: 13372
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b-D-Galp-(1-6)-+
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b-D-Galp-(1-3)-+ |
| |
b-D-Galp-(1-2)-a-D-Rhap-(1-4)-+ |
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-3)-a-D-Glcp-(1-3)-a-D-GlcpA-(1-3)-a-D-Manp-(1-
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a-D-Galp-(1-2)-+ |
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Structure type: polymer chemical repeating unit
Compound class: EPS, galactoglucomannan
Reference(s) to other database(s): GTC:G46506QX
- Compound ID: 19469
Structure type: polymer chemical repeating unit
; n=111, 36000
Compound class: EPS, galactoglucan, glucogalactan
Reference(s) to other database(s): GTC:G25521ED
- Compound ID: 19468
|
b-D-Galf-(1-6)-+ b-D-Manp-(1-6)-a-D-Manp-(1-6)-+ b-D-Manp-(1-6)-+
| | |
-2)-a-D-Manp-(1-2)-a-D-Manp-(1-2)-a-D-Manp-(1-2)-a-D-Manp-(1-2)-a-D-Manp-(1-2)-a-D-Manp-(1-2)-a-D-Manp-(1-2)-a-D-Manp-(1-2)-a-D-Manp-(1- |
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Structure type: structural motif or average structure
; n=7, 15000
Compound class: EPS, galactomannan
Reference(s) to other database(s): GTC:G23072GV
- Compound ID: 19470
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a-L-Rhap-(1-6)-+
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-2)-a-L-Rhap-(1-4)-b-D-Galp-(1-4)-b-D-Galp-(1-4)-b-D-Galp-(1-4)-b-D-Galp-(1- |
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Structure type: structural motif or average structure
; n=178, 187000
Compound class: EPS, rhamnogalactan
Reference(s) to other database(s): GTC:G29057YX
- Compound ID: 19467
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b-D-Galf-(1-5)-{{{-b-D-Galf-(1-5)-}}}/n=0-7/-b-D-Galf-(1-6)-+
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a-D-Manp-(1-6)-+ |
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a-D-Manp-(1-6)-+ | |
| | |
-2)-a-D-Manp-(1-2)-a-D-Manp-(1-2)-a-D-Manp-(1-2)-a-D-Manp-(1-2)-a-D-Manp-(1- |
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Structure type: structural motif or average structure
; n=16, 29000
Compound class: EPS, galactomannan
- Compound ID: 19471
Structure type: homopolymer
; 200000
Compound class: EPS, glucan
Reference(s) to other database(s): GTC:G51056AN
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2. (Article ID: 8180)
Guo S, Mao W, Yan M, Zhao C, Li N, Shan J, Lin C, Liu X, Guo T, Wang S
Galactomannan with novel structure produced by the coral endophytic fungus Aspergillus ochraceus
Carbohydrate Polymers 105 (2014)
325–333
The homogeneous extracellular polysaccharide, AW1, was obtained from the fermented broth of the fungus Aspergillus ochraceus derived from coral Dichotella gemmacea. AW1 was a galactomannan with a molar ratio of mannose and galactose of 2.16:1.00 and a molecular weight of about 29.0kDa. The structure of AW1 was investigated by chemical and spectroscopic methods, including methylation analysis, one- and two-dimensional nuclear magnetic resonance (1D, 2D NMR) and electrospray mass spectrometry with collision-induced dissociation (ES-CID MS/MS) spectroscopic analyses. The results showed that the backbone of AW1 consisted of (1⟶2)-linked α-d-mannopyranose residues. The mannopyranose residues in the backbone were substituted at C-6 by the (1⟶)-linked α-d-mannopyranose units and (1⟶5)-linked β-D-galactofuranose oligosaccharides with different degrees of polymerization. The investigation demonstrated that AW1 was a novel galactomannan with different structural characteristics from other fungal galactomannans, and could be a potential resource of the (1⟶5)-linked β-D-galactofuranose oligosaccharides.
NMR, extracellular polysaccharide, Aspergillus ochraceus, ES-CID MS/MS, galacto-oligosaccharide
NCBI PubMed ID: 24708987Publication DOI: 10.1016/j.carbpol.2014.01.079Journal NLM ID: 8307156Publisher: Elsevier
Correspondence: Mao W
hotmail.com>
Institutions: Key Laboratory of Marine Drugs, Ministry of Education, School of Medicine and Pharmacy, Ocean University of China, Qingdao, China, Key Laboratory of Atherosclerosis in Universities of Shandong Province, Institute of Atherosclerosis, Taishan Medical University, Taian, Shandong, China
Methods: 13C NMR, 1H NMR, IR, GC-MS, ESI-MS, ESI-MS/MS, GC, HPLC, FPLC, methylation analysis, reduction with NaBH4, ESI-CID-MS/MS, HPGPC, phenol-sulfuric acid assay, HMBC, Bradford method, HMQC, DEPT, COSY, NOESY, HCl hydrolysis, TFA hydrolysis, HP-TLC, Hakamori method
The publication contains the following compound(s):
- Compound ID: 20553
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b-D-Galf-(1-5)-b-D-Galf-(1-5)-b-D-Galf-(1-5)-b-D-Galf-(1-5)-D-Galf |
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Structure type: oligomer
; 829.5 [M+H]+
Compound class: galactan
Reference(s) to other database(s): GTC:G68891VQ
- Compound ID: 20554
|
b-D-Galf-(1-5)-{{{-b-D-Galf-(1-5)-}}}/n=0-7/-b-D-Galf-(1-6)-+
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a-D-Manp-(1-6)-+ |
| |
a-D-Manp-(1-6)-+ | |
| | |
-2)-a-D-Manp-(1-2)-a-D-Manp-(1-2)-a-D-Manp-(1-2)-a-D-Manp-(1-2)-a-D-Manp-(1- |
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Structure type: structural motif or average structure
; 29000, n=16
Compound class: galactomannan
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